Bhattacharya R K, Firozi P F, Aboobaker V S
Carcinogenesis. 1984 Oct;5(10):1359-62. doi: 10.1093/carcin/5.10.1359.
Forty-two compounds belonging to various chemical groups have been tested for their ability to suppress formation of aflatoxin B1--DNA adduct mediated by microsome in vitro. While many of these compounds have either marginal or no modulating effect, some have been identified as effective inhibitors. The strong inhibition of DNA adduct formation by retinoids (retinol, retinal, retinoic acid and retinyl acetate), riboflavin, riboflavin 5'-phosphate, flavin adenine dinucleotide, Cu2+, 7,8-benzoflavone, disulfiram, butylated hydroxyanisole, butylated hydroxytoluene and phenothiazine suggests that these agents may have potential anticarcinogenic activity against aflatoxin B1.
对42种属于不同化学类别的化合物进行了测试,以检测它们在体外抑制由微粒体介导的黄曲霉毒素B1-DNA加合物形成的能力。虽然这些化合物中的许多要么具有微弱的调节作用,要么没有调节作用,但有些已被确定为有效的抑制剂。视黄醇(视黄醇、视黄醛、视黄酸和醋酸视黄酯)、核黄素、核黄素5'-磷酸、黄素腺嘌呤二核苷酸、铜离子、7,8-苯并黄酮、双硫仑、丁基羟基茴香醚、丁基化羟基甲苯和吩噻嗪对DNA加合物形成的强烈抑制作用表明,这些试剂可能对黄曲霉毒素B1具有潜在的抗癌活性。